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Hypokinesia clinical trials

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NCT ID: NCT00657501 Completed - Clinical trials for Hypoactive Sexual Desire Disorder

Safety and Efficacy of LibiGel® for Treatment of Hypoactive Sexual Desire Disorder in Surgically Menopausal Women

BLOOM
Start date: March 2008
Phase: Phase 3
Study type: Interventional

This study is a randomized, double-blind, placebo-controlled, multi-center study of the safety and efficacy of LibiGel 300mcg in the treatment of HSDD in surgically menopausal women.

NCT ID: NCT00613002 Completed - Clinical trials for Hypoactive Sexual Desire Disorder

Safety and Efficacy of LibiGel® for the Treatment of Hypoactive Sexual Desire Disorder in Surgically Menopausal Women

BLOOM
Start date: December 2006
Phase: Phase 3
Study type: Interventional

This study is a randomized, double-blind, placebo-controlled, multi-center study of the safety and efficacy of LibiGel® 300mcg in the treatment of HSDD in surgically menopausal women

NCT ID: NCT00612742 Completed - Clinical trials for Hypoactive Sexual Desire Disorder

Safety and Efficacy of LibiGel® for Treatment of Hypoactive Sexual Desire Disorder in Postmenopausal Women

BLOOM
Start date: January 2008
Phase: Phase 3
Study type: Interventional

This study is a randomized, double-blind, placebo-controlled, adaptive design, multi-center study of the long-term cardiovascular and breast safety of LibiGel in the treatment of HSDD in postmenopausal women with at least two points of cardiovascular risk and clinical diagnosis of Hypoactive Sexual Desire Disorder (HSDD).

NCT ID: NCT00599287 Terminated - Delirium Clinical Trials

Methylphenidate, Rivastigmine or Haloperidol in Hypoactive Delirium in Intensive Care Patients

Start date: February 2008
Phase: Phase 3
Study type: Interventional

The purpose of this pilot-trial is the feasibility of a large randomized, placebo controlled, doubleblind clinical trial to investigate the use of methylphenidate, rivastigmine or haloperidol in hypoactive ICU-delirium. In addition we will compare duration of delirium, severity of delirium, length of ICU/hospital stay and side effects between the different interventions.

NCT ID: NCT00551785 Terminated - Hysterectomy Clinical Trials

Surveillance Study of Women Taking Intrinsa®

EMPOWER
Start date: September 2007
Phase: Phase 4
Study type: Observational

The primary objective of the study is to assess the risks of testosterone transdermal patch use in a representative study population. The primary clinical outcome of interest is breast cancer.

NCT ID: NCT00467259 Completed - Clinical trials for Hypoactive Sexual Desire Disorder

Endometrial Safety Study of Transdermal Testosterone (300 Mcg/Day) in Naturally Postmenopausal Women

Start date: April 2007
Phase: Phase 3
Study type: Interventional

This study is designed to evaluate the endometrial safety of a testosterone patch as treatment for low libido in naturally postmenopausal women.

NCT ID: NCT00441428 Completed - Overactive Bladder Clinical Trials

Safety And Efficacy Of Solifenacin In Men With Overactive Bladder (OAB) And Detrusor Underactivity

Start date: February 2006
Phase: Phase 2
Study type: Observational

Detrusor underactivity (DUA) in men is responsible for LUTS in a significant minority, the symptoms being indistinguishable from those seen in BOO. The International Continence Society (ICS) defines DUA as 'a detrusor contraction of inadequate magnitude and/or duration to effect complete bladder emptying in the absence of urethral obstruction. Whilst a reduced maximum urinary flow rate (Qmax) is indicative of voiding dysfunction, flow studies cannot distinguish between DUA and BOO, which are the two principal causes of low flow rates. DUA is diagnosed from a pressure-flow study (PFS)and is characterized by a low-pressure, poorly sustained, or wave-like detrusor contraction with an associated poor flow rate. Overactive bladder (OAB) is the most common term currently used in clinical medicine to describe a complex of lower urinary tract symptoms (LUTS) with or without incontinence but most commonly consisting of urgency, frequency, nocturia, troublesome or incomplete emptying,and, occasionally, pain. With the exception of pain and incontinence, these symptoms are often found together; thus, the term LUTS has come to replace previous terms, such as urgency-frequency syndrome,urethral syndrome, and prostatism. Drug treatment is frequently used as the initial management approach for LUTS in older men.Among men who desire treatment, general practice prescribing data have shown that antimuscarinics are not often given to elderly men. There is theoretical concern that the inhibitory effect of antimuscarinics on detrusor contraction could aggravate voiding difficulties or cause urinary retention in patients with BOO. There are virtually no data evaluating the safety and efficacy of solifenacin treatment in men with DUA and OAB.

NCT ID: NCT00384046 Completed - Clinical trials for Hypoactive Sexual Desire Disorder

Testosterone Therapy in Naturally Menopausal Women With Low Sexual Desire Receiving Transdermal Estrogen

Start date: November 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to examine whether the transdermal testosterone system (TTS) is effective and safe in the treatment of hypoactive sexual desire disorder (HSDD) in postmenopausal women who are on transdermal estrogen.

NCT ID: NCT00349791 Completed - Clinical trials for Hypoactive Sexual Desire Disorder (HSDD)

Study to Assess the Efficacy/Safety of Transdermal Testosterone Patches in Naturally Menopausal Women With Low Libido

Start date: June 2002
Phase: Phase 3
Study type: Interventional

This study is designed to evaluate efficacy and safety of a testosterone patch as treatment for low libido in naturally menopausal women who are taking estrogen or estrogen/progestin therapy.

NCT ID: NCT00338312 Completed - Clinical trials for Hypoactive Sexual Desire Disorder

Study of Transdermal Testosterone Patches in Naturally Menopausal Women With Low Libido

Start date: June 2002
Phase: Phase 3
Study type: Interventional

This study is designed to evaluate efficacy and safety of a testosterone patch as treatment for low libido in naturally menopausal women who are taking estrogen or estrogen/progestin therapy.